|
MIM:245900 - LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
Xenbase Genes: lcat
Human Disease Resource: MIM
| MONDO:0009515 - Norum disease |
| MONDO:0018999 - LCAT deficiency |
| DOID:1391 - Norum disease |
|
| MONDO:0009515 - Norum disease |
| MONDO:0018999 - LCAT deficiency |
| DOID:1391 - Norum disease |